Works about THIOUREA
Results: 2147
Thiosemicarbazone- and Thiourea-Functionalized Calix[4]arenes in cone and 1,3- alternate Conformations: Receptors for the Recognition of Ions.
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- Chemosensors, 2025, v. 13, n. 2, p. 48, doi. 10.3390/chemosensors13020048
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Two-Dimensional Carbon Film-Supported ZnS Nanocomposites Obtained from Thermal Decomposition of Organic Zinc Salts and Sulfidation Reactions for Lithium Storage.
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- Molecules, 2025, v. 30, n. 4, p. 893, doi. 10.3390/molecules30040893
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Thioureas Derived from (S)-1-(2-pyridyl)ethylamine Enantiomer: Synthesis and Selected Applications as an Organocatalyst.
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- Symmetry (20738994), 2025, v. 17, n. 2, p. 216, doi. 10.3390/sym17020216
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- Article
SYNTHESIS AND TRANSFORMATIONS OF 3-AMINO-3H-SPIRO[BENZO[h]QUINAZOLINE-5,1'- CYCLOHEPTAN]-4(6H)-ONE.
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- Electronic Journal of Natural Sciences, 2021, v. 36, n. 1, p. 26
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Thioureas Bridged Polysiloxanes for Ultrafast Detection of Cr<sup>6+</sup> and Applications.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 13, p. 1, doi. 10.1002/macp.202100080
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A New Two‐Step Strategy for Encapsulating Amorphous Polymer Chains in Thiourea Crystals.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 20, p. 1, doi. 10.1002/macp.202000269
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Ionic (Co)Organocatalyst with (Thio)Urea Anion and Tetra‑n‑butyl Ammonium Cation for the Polymerization of γ‐Butyrolactone.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 16, p. 1, doi. 10.1002/macp.202000172
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Asymmetric Kinetic Resolution Polymerization of Racemic Lactide Mediated by Axial‐Chiral Thiourea/Phosphazene Binary Organocatalyst.
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- Chemistry - A European Journal, 2024, v. 30, n. 53, p. 1, doi. 10.1002/chem.202402201
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Mesoionic Janus‐Type Dicarbene: Complexes, Adducts, and Catalytic Studies.
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- Chemistry - A European Journal, 2024, v. 30, n. 51, p. 1, doi. 10.1002/chem.202402127
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- Article
Unlocking Photocatalytic Activity of Acridinium Salts by Anion‐Binding Co‐Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202400541
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- Article
Sulfur‐ and Amine‐ Promoted Multielectron Autoredox Transformation of Nitromethane: Multicomponent Access to Thiourea Derivatives.
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- Chemistry - A European Journal, 2024, v. 30, n. 7, p. 1, doi. 10.1002/chem.202303703
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Optimization of a 1,4,7‐Triazacyclononane‐1,4‐diacetic acid (NODA) Derivative Radiofluorination by Al<sup>18</sup>F Complexation Using a Design of Experiments Approach.
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- Chemistry - A European Journal, 2023, v. 29, n. 71, p. 1, doi. 10.1002/chem.202302745
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Organocatalyzed Regioselective Synthesis of 1,5‐Disubstituted 1,2,3‐Triazolyl Glycoconjugates.
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- Chemistry - A European Journal, 2023, v. 29, n. 55, p. 1, doi. 10.1002/chem.202301749
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- Article
A Cu<sup>+</sup>/Thiourea Dendrimer Achieves Excellent Cytosolic Protein Delivery via Enhanced Cell Uptake and Endosome Escape.
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- Chemistry - A European Journal, 2023, v. 29, n. 22, p. 1, doi. 10.1002/chem.202300131
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[ReH<sub>3</sub>(PPh<sub>3</sub>)<sub>4</sub>] – A Key Compound in the Rhenium Hydride Chemistry.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203317
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Synthesis of Sterically Encumbered Thiourea S‐Oxides through Direct Thiourea Oxidation.
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- Chemistry - A European Journal, 2023, v. 29, n. 4, p. 1, doi. 10.1002/chem.202203005
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Synthesis of Metal Chalcogenide Semiconductors by Thermal Decomposition of Organosulfur and Organoselenium Compounds.
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- Chemistry - A European Journal, 2022, v. 28, n. 61, p. 1, doi. 10.1002/chem.202201951
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Copper‐Catalyzed Regioselective [3+3] Annulations of Alkynyl Ketimines with α‐Cyano Ketones: the Synthesis of Polysubstituted 4H‐Pyran Derivatives with a CF<sub>3</sub>‐Containing Quaternary Center.
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- Chemistry - A European Journal, 2022, v. 28, n. 23, p. 1, doi. 10.1002/chem.202200128
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Thiourea‐ and Amino‐Substituted Benzoxadiazole Dyes with Large Stokes Shifts as Red‐Emitting Probe Monomers for Imprinted Polymer Layers Targeting Carboxylate‐Containing Antibiotics.
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- Chemistry - A European Journal, 2022, v. 28, n. 21, p. 1, doi. 10.1002/chem.202104525
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Catalytic Enantioselective Biltz Synthesis.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202313797
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Turning on the Antimicrobial Activity of Gold Nanoclusters Against Multidrug‐Resistant Bacteria.
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- Angewandte Chemie, 2023, v. 135, n. 11, p. 1, doi. 10.1002/ange.202214086
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- Article
A Desilylative Approach to Alkyl Substituted C(1)‐Ammonium Enolates: Application in Enantioselective [2+2] Cycloadditions.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202208800
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Tug‐of‐War between Two Distinct Catalytic Sites Enables Fast and Selective Ring‐Opening Copolymerizations.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202208525
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Photoredox Generation of Isothiouronyl Radical Cations: A New Platform in Covalent Radical Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205596
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London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202204393
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Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202202621
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Rational Design of Axially Chiral Styrene‐Based Organocatalysts and Their Application in Catalytic Asymmetric (2+4) Cyclizations.
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- Angewandte Chemie, 2022, v. 134, n. 7, p. 1, doi. 10.1002/ange.202112226
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Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Iridium and Chiral Thiourea Sequential Catalysis.
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 8909, doi. 10.1002/ange.202015898
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Enantio‐ and Diastereoselective Nucleophilic Addition of N‐tert‐Butylhydrazones to Isoquinolinium Ions through Anion‐Binding Catalysis.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 5156, doi. 10.1002/ange.202012861
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Design and Atroposelective Construction of IAN analogues by Organocatalytic Asymmetric Heteroannulation of Alkynes.
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- Angewandte Chemie, 2020, v. 132, n. 51, p. 23277, doi. 10.1002/ange.202010598
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Enantioselective Syntheses of Strychnos and Chelidonium Alkaloids through Regio‐ and Stereocontrolled Cooperative Catalysis.
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- Angewandte Chemie, 2020, v. 132, n. 40, p. 17709, doi. 10.1002/ange.202005151
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Isothiourea‐Catalyzed Acylative Kinetic Resolution of Tertiary α‐Hydroxy Esters.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16715, doi. 10.1002/ange.202004354
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Substrate‐Induced Dimerization Assembly of Chiral Macrocycle Catalysts toward Cooperative Asymmetric Catalysis.
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- Angewandte Chemie, 2020, v. 132, n. 7, p. 2645, doi. 10.1002/ange.201910399
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- Article
Base‐free Enantioselective C(1)‐Ammonium Enolate Catalysis Exploiting Aryloxides: A Synthetic and Mechanistic Study.
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- Angewandte Chemie, 2019, v. 131, n. 42, p. 15255, doi. 10.1002/ange.201908627
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Dissipative Catalysis with a Molecular Machine.
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- Angewandte Chemie, 2019, v. 131, n. 29, p. 9981, doi. 10.1002/ange.201907113
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Chiral Brønsted Acid Catalyzed Dynamic Kinetic Asymmetric Hydroamination of Racemic Allenes and Asymmetric Hydroamination of Dienes.
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- Angewandte Chemie, 2019, v. 131, n. 21, p. 7166, doi. 10.1002/ange.201900955
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Achiral Trisubstituted Thioureas as Secondary Ligands to Cu<sup>I</sup> Catalysts: Direct Catalytic Asymmetric Addition of α‐Fluoronitriles to Imines.
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- Angewandte Chemie, 2019, v. 131, n. 9, p. 2670, doi. 10.1002/ange.201812673
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Access to All‐Carbon Spirocycles through a Carbene and Thiourea Cocatalytic Desymmetrization Cascade Reaction.
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- Angewandte Chemie, 2019, v. 131, n. 6, p. 1798, doi. 10.1002/ange.201810638
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Efficient Sb<sub>2</sub>S<sub>3</sub>-Sensitized Solar Cells Via Single-Step Deposition of Sb<sub>2</sub>S<sub>3</sub> Using S/Sb-Ratio-Controlled SbCl<sub>3</sub>-Thiourea Complex Solution.
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- Advanced Functional Materials, 2015, v. 25, n. 19, p. 2892, doi. 10.1002/adfm.201500296
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Sensory Arrays of Covalently Functionalized Single-Walled Carbon Nanotubes for Explosive Detection.
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- Advanced Functional Materials, 2014, v. 23, n. 42, p. 5285, doi. 10.1002/adfm.201300131
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Synthesis of thioesters and thioamides under solvothermal condition using thiourea as thionating agent.
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- Journal of Materials Science, 2006, v. 41, n. 5, p. 1391, doi. 10.1007/s10853-006-7412-z
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- Article
Quantitative Raman Spectroscopy of Urea and Thiourea in the Reaction Mixtures of Allantoin and 4,5‐Dihydroxyimidazolidine‐2‐Tione Formation.
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- Journal of Raman Spectroscopy, 2024, v. 55, n. 11, p. 1165, doi. 10.1002/jrs.6729
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Darling-Dennison resonance of thiourea adsorbed on the silver electrode revealed by surface enhanced Raman spectroscopy.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 9, p. 1273, doi. 10.1002/jrs.4358
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1-Phenyl-3-(2-thiazolyl)-2-thiourea inhibits melanogenesis via a dual-action mechanism.
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- Archives of Dermatological Research, 2016, v. 308, n. 7, p. 473, doi. 10.1007/s00403-016-1659-2
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Synthesis and Investigation of the Antibacterial Activity of New Tris-Thiourea Derivatives.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 1, p. 60, doi. 10.1007/s11094-021-02372-6
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- Article
Synthesis and Analgesic Activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 4, p. 226, doi. 10.1007/s11094-016-1427-9
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Synthesis and Pharmacological Activity of 2,9-Disubstituted Imidazo[1,2- a]Benzimidazole Phenyl- and Alkylthiocarbamides.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 10, p. 653, doi. 10.1007/s11094-016-1346-9
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Synthesis and Antioxidant Activity of 2-Thioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbamides.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 4, p. 246, doi. 10.1007/s11094-014-1087-6
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Synthesis of 4-Aryl(Hetaryl)Spinaceamine Thioureas.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 2, p. 89, doi. 10.1007/s11094-014-1054-2
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Synthesis and antimicrobial activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 2, p. 114, doi. 10.1007/s11094-012-0743-y
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